Works matching DE "CYCLOPROPENE"
Results: 115
Synthesis of Cyclopropenes and Fluorinated Cyclopropanes via Michael Initiated Ring Closure of Alkyl Triflones.
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- Chemistry - A European Journal, 2022, v. 28, n. 23, p. 1, doi. 10.1002/chem.202104364
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Enantioselective Total Synthesis of (+)‐Eucophylline.
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- Chemistry - A European Journal, 2022, v. 28, n. 16, p. 1, doi. 10.1002/chem.202200088
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Photocatalytic Decarboxylative Functionalization of Cyclopropenes via Cyclopropenium Cation Intermediates.
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- Angewandte Chemie, 2024, v. 136, n. 32, p. 1, doi. 10.1002/ange.202404265
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Heavy‐Atom Tunneling in Bicyclo[4.1.0]hepta‐2,4,6‐trienes.
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- Angewandte Chemie, 2023, v. 135, n. 44, p. 1, doi. 10.1002/ange.202309717
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Copper(I)‐Catalyzed Asymmetric Hydrophosphination of 3,3‐Disubstituted Cyclopropenes.
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- Angewandte Chemie, 2023, v. 135, n. 40, p. 1, doi. 10.1002/ange.202218798
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Late‐Stage Aryl C−H Bond Cyclopropenylation with Cyclopropenium Cations.
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- Angewandte Chemie, 2023, v. 135, n. 36, p. 1, doi. 10.1002/ange.202308379
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Diastereo‐ and Enantioselective Hydrophosphination of Cyclopropenes under Lanthanocene Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 34, p. 1, doi. 10.1002/ange.202308488
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Cobalt‐Catalyzed Facial‐Selective Hydroalkylation of Cyclopropenes.
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- Angewandte Chemie, 2023, v. 135, n. 30, p. 1, doi. 10.1002/ange.202306381
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Diboron(4)‐Catalyzed Remote [3+2] Cycloaddition of Cyclopropanes via Dearomative/Rearomative Radical Transmission through Pyridine.
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- Angewandte Chemie, 2022, v. 134, n. 52, p. 1, doi. 10.1002/ange.202214507
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(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202209006
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Metal‐Free Ring‐Opening Metathesis Polymerization with Hydrazonium Initiators**.
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202203344
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Dearomative Cyclopropanation of Naphthols via Cyclopropene Ring‐Opening.
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- Angewandte Chemie, 2022, v. 134, n. 8, p. 1, doi. 10.1002/ange.202116171
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Directed Regioselective Carbometallation of 1,2‐Dialkyl‐Substituted Cyclopropenes.
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- Angewandte Chemie, 2021, v. 133, n. 50, p. 26572, doi. 10.1002/ange.202111382
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Regio‐ and Diastereoselective Copper‐Catalyzed Carbomagnesiation for the Synthesis of Penta‐ and Hexa‐Substituted Cyclopropanes.
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- Angewandte Chemie, 2021, v. 133, n. 21, p. 11910, doi. 10.1002/ange.202102509
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Enantioselective Synthesis of 3,3′‐Disubstituted 2‐Amino‐2′‐hydroxy‐1,1′‐binaphthyls by Copper‐Catalyzed Aerobic Oxidative Cross‐Coupling.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7137, doi. 10.1002/ange.202015001
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Azide Radical Initiated Ring Opening of Cyclopropenes Leading to Alkenyl Nitriles and Polycyclic Aromatic Compounds.
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- Angewandte Chemie, 2021, v. 133, n. 8, p. 4121, doi. 10.1002/ange.202013516
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Cobalt‐Catalyzed Diastereo‐ and Enantioselective Hydroalkylation of Cyclopropenes with Cobalt Homoenolates.
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- Angewandte Chemie, 2021, v. 133, n. 5, p. 2726, doi. 10.1002/ange.202012122
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Selective Alkynylallylation of the C−C σ Bond of Cyclopropenes.
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- Angewandte Chemie, 2021, v. 133, n. 1, p. 301, doi. 10.1002/ange.202008886
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Tuning the Reactivity of Cyclopropenes from Living Ring‐Opening Metathesis Polymerization (ROMP) to Single‐Addition and Alternating ROMP.
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- Angewandte Chemie, 2019, v. 131, n. 49, p. 17935, doi. 10.1002/ange.201909688
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Catalytic Desymmetric Cycloaddition of Diaziridines with Metalloenolcarbenes: The Role of Donor–Acceptor Cyclopropenes.
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- Angewandte Chemie, 2019, v. 131, n. 36, p. 12632, doi. 10.1002/ange.201906754
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A Cyclopropene Electrophile that Targets Glutathione S‐Transferase Omega‐1 in Cells.
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- Angewandte Chemie, 2019, v. 131, n. 34, p. 12044, doi. 10.1002/ange.201907520
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Cobalt‐Catalyzed Diastereo‐ and Enantioselective Hydroalkenylation of Cyclopropenes with Alkenylboronic Acids.
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- Angewandte Chemie, 2019, v. 131, n. 32, p. 11165, doi. 10.1002/ange.201904994
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Synthesis and Characterization of Cyclopropaosmanaphthalenes Containing a Fused σ‐Aromatic Metallacyclopropene Unit.
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- Angewandte Chemie, 2019, v. 131, n. 27, p. 9272, doi. 10.1002/ange.201904815
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[(NHC)Ni<sup>II</sup>H]‐Catalyzed Cross‐Hydroalkenylation of Cyclopropenes with Alkynes: Cyclopentadiene Synthesis by [(NHC)Ni<sup>II</sup>]‐Assisted C−C Rearrangement.
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- Angewandte Chemie, 2019, v. 131, n. 17, p. 5758, doi. 10.1002/ange.201901255
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Innenrücktitelbild: Multi‐Light‐Responsive Quantum Dot Sensitized Hybrid Micromotors with Dual‐Mode Propulsion (Angew. Chem. 10/2019).
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3261, doi. 10.1002/ange.201901669
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Rücktitelbild: Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair (Angew. Chem. 10/2019).
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3262, doi. 10.1002/ange.201901616
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Titelbild: Disorder Engineering in Monolayer Nanosheets Enabling Photothermic Catalysis for Full Solar Spectrum (250–2500 nm) Harvesting (Angew. Chem. 10/2019).
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 2933, doi. 10.1002/ange.201900971
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Innentitelbild: EPR Spectroscopy Detects Various Active State Conformations of the Transcriptional Regulator CueR (Angew. Chem. 10/2019).
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 2934, doi. 10.1002/ange.201900968
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Zugang zu 1‐Phospha‐2‐azanorbornenen durch Phospha‐Aza‐Diels‐Alder‐Reaktionen.
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3240, doi. 10.1002/ange.201811673
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Synthetic strategies towards the carbenoid reactions of α;β-acetylenic carbonyls.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 5, p. 1384, doi. 10.3906/kim-1805-65
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Determination of Nutritional and Cyclopropenoid Fatty Acids in Cottonseed by a Single GC Analysis.
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- Journal of the American Oil Chemists' Society (JAOCS), 2015, v. 92, n. 7, p. 947, doi. 10.1007/s11746-015-2669-5
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Fatty Acid Profile of Kenaf Seed Oil.
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- Journal of the American Oil Chemists' Society (JAOCS), 2013, v. 90, n. 6, p. 835, doi. 10.1007/s11746-013-2230-3
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Isolable Si=B Analogue of a Vinyl Halide: A Building Block for Facile Access toward Silicon‐Boron Multiple Bonded Species.
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- Angewandte Chemie, 2024, v. 136, n. 47, p. 1, doi. 10.1002/ange.202411283
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Stereoselective Hydroxyallylation of Cyclopropenes with Cyclopropanols via NHC Catalysis of Transient Organozinc Species.
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- Angewandte Chemie, 2024, v. 136, n. 46, p. 1, doi. 10.1002/ange.202412456
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From Cyclopropene to Housane Derivatives Via Intramolecular Cyclopropanation.
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- Angewandte Chemie, 2024, v. 136, n. 46, p. 1, doi. 10.1002/ange.202409226
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The combined CASPT2 and CASSCF studies on photolysis of 3-thienyldiazomethane and subsequent reactions.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2014, v. 133, n. 9, p. 1, doi. 10.1007/s00214-014-1532-3
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A neglected aspect of the puzzle of chemical structure: how history helps.
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- Foundations of Chemistry, 2012, v. 14, n. 3, p. 235, doi. 10.1007/s10698-012-9146-0
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Cobalt‐Catalyzed Diastereo‐ and Enantioselective Hydroarylation of Cyclopropenes with Arylboronic Acids.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 3, p. 1, doi. 10.1002/ajoc.202200720
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Synthetic Applications of Cyclopropene and Cyclopropenone: Recent Progress and Developments.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 8, p. 1088, doi. 10.1002/ajoc.202000193
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Small‐Ring Metathesis: Delights and Difficulties.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 12, p. 2386, doi. 10.1002/ajoc.201800515
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NHC-Ni(II)-catalyzed cyclopropene-isocyanide [5 + 1] benzannulation.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31896-y
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Front Cover: σ‐Aromaticity in a Fully Unsaturated Ring (Chem. Asian J. 23/2018).
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- Chemistry - An Asian Journal, 2018, v. 13, n. 23, p. 3554, doi. 10.1002/asia.201801562
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σ‐Aromaticity in a Fully Unsaturated Ring.
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- Chemistry - An Asian Journal, 2018, v. 13, n. 23, p. 3691, doi. 10.1002/asia.201801279
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Silver-Catalyzed Allylation of Ketones and Intramolecular Cyclization through Carbene Intermediates from Cyclopropenes Under Ambient Conditions.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 5, p. 713, doi. 10.1002/asia.201501196
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DFT study on the regio- and stereo-selectivity of the Diels-Alder reaction between a cycloprop-2-ene carboxylate and some cyclic 1,3-dienes.
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- Progress in Reaction Kinetics & Mechanism, 2016, v. 41, n. 2, p. 193, doi. 10.3184/146867816X14636767119354
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Divergent Annulations of 5,6‐Dihydro‐4H‐1,2‐Oxazine N‐Oxides and Enol Diazoacetates for the Switchable Chemoselective Synthesis of Fused 1,2‐Oxazine Derivatives.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 45, p. 1, doi. 10.1002/ejoc.202400768
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Synthesis of a CF<sub>3</sub>-substituted 1,3,4-oxadiazoline and its use in the generation and trapping of an α-trifluoromethyl carbene.
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- ARKIVOC: Online Journal of Organic Chemistry, 2024, v. 2024, p. 1, doi. 10.24820/ark.5550190.p012.164
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An improved synthesis of a cyclopropene-based molecule for the fabrication of bioengineered tissues via copper-free click chemistry.
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- Journal of Applied Biomaterials & Functional Materials, 2019, v. 17, n. 2, p. N.PAG, doi. 10.1177/2280800019844746
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Storage Stability of Nutritional Qualities, Enzyme Activities, and Volatile Compounds of "Hangjiao No. 2" Chili Pepper Treated With Different Concentrations of 1-Methyl Cyclopropene.
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- Frontiers in Plant Science, 2022, v. 13, p. 1, doi. 10.3389/fpls.2022.838916
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Mechanistic Insights into the Rh(I)/Rh<sub>2</sub>(II)‐Catalyzed Divergent Ring‐Opening of Cyclopropenes: A Computational Study.
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- ChemCatChem, 2020, v. 12, n. 22, p. 5656, doi. 10.1002/cctc.202001149
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